Journal article
Mechanistic Studies on Norcoclaurine Synthase of Benzylisoquinoline Alkaloid Biosynthesis: An Enzymatic Pictet−Spengler Reaction †
Abstract
Norcoclaurine synthase catalyzes an asymmetric Pictet-Spengler condensation of dopamine and 4-hydroxyphenylacetaldehyde to give (S)-norcoclaurine. This is the first committed step in the biosynthesis of the benzylisoquinoline alkaloids that include morphine and codeine. In this work, the gene encoding for the Thalictrum flavum norcoclaurine synthase is highly overexpressed in Escherichia coli and the resulting His-tagged recombinant enzyme is …
Authors
Luk LYP; Bunn S; Liscombe DK; Facchini PJ; Tanner ME
Journal
Biochemistry, Vol. 46, No. 35, pp. 10153–10161
Publisher
American Chemical Society (ACS)
Publication Date
September 1, 2007
DOI
10.1021/bi700752n
ISSN
0006-2960